Dimensional Control of Block Copolymer Nanofibers with a π‐Conjugated Core: Crystallization‐Driven Solution Self‐Assembly of Amphiphilic Poly(3‐hexylthiophene)‐b‐poly(2‐vinylpyridine) |
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| Authors: | Dr. Jessica Gwyther Prof. Joe B. Gilroy Prof. Paul A. Rupar David J. Lunn Emily Kynaston Prof. Sanjib K. Patra Dr. George R. Whittell Prof. Mitchell A. Winnik Prof. Ian Manners |
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| Affiliation: | 1. School of Chemistry, University of Bristol, Bristol BS8 1TS (UK);2. Current Address: Department of Chemistry, The University of Western Ontario, London 3. ON, N6A 5B7 (Canada);4. Current Address: Department of Chemistry, The University of Alabama, Tuscaloosa AL, 35487 (USA);5. Current Address: Department of Chemistry, Indian Institute of Technology, Kharagpur, 721302 (India);6. Department of Chemistry, University of Toronto, Toronto ON, M5S 3H6 (Canada) |
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| Abstract: | With the aim of accessing colloidally stable, fiberlike, π‐conjugated nanostructures of controlled length, we have studied the solution self‐assembly of two asymmetric crystalline–coil, regioregular poly(3‐hexylthiophene)‐b‐poly(2‐vinylpyridine) (P3HT‐b‐P2VP) diblock copolymers, P3HT23‐b‐P2VP115 (block ratio=1:5) and P3HT44‐b‐P2VP115 (block ratio=ca. 1:3). The self‐assembly studies were performed under a variety of solvent conditions that were selective for the P2VP block. The block copolymers were prepared by using Cu‐catalyzed azide–alkyne cycloaddition reactions of azide‐terminated P2VP and alkyne end‐functionalized P3HT homopolymers. When the block copolymers were self‐assembled in a solution of a 50 % (v/v) mixture of THF (a good solvent for both blocks) and an alcohol (a selective solvent for the P2VP block) by means of the slow evaporation of the common solvent; fiberlike micelles with a P3HT core and a P2VP corona were observed by transmission electron microscopy (TEM). The average lengths of the micelles were found to increase as the length of the hydrocarbon chain increased in the P2VP‐selective alcoholic solvent (MeOH<iPrOH<nBuOH). Very long (>3 μm) fiberlike micelles were prepared by the dialysis of solutions of the block copolymers in THF against iPrOH. Furthermore the widths of the fibers were dependent on the degree of polymerization of the chain‐extended P3HT blocks. The crystallinity and π‐conjugated nature of the P3HT core in the fiberlike micelles was confirmed by a combination of UV/Vis spectroscopy, photoluminescence (PL) measurements, and wide‐angle X‐ray scattering (WAXS). Intense sonication (iPrOH, 1 h, 0 °C) of the fiberlike micelles formed by P3HT23‐b‐P2VP115 resulted in small (ca. 25 nm long) stublike fragments that were subsequently used as initiators in seeded growth experiments. Addition of P3HT23‐b‐P2VP115 unimers to the seeds allowed the preparation of fiberlike micelles with narrow length distributions (Lw/Ln <1.11) and lengths from about 100‐300 nm, that were dependent on the unimer‐to‐seed micelle ratio. |
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| Keywords: | block copolymers micelles nanowires self‐assembly |
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